Toughening of Glassy Supramolecular Polymer Networks
Author(s) -
Diana Kay Hohl,
AnneCécile Ferahian,
Lucas Montero de Espinosa,
Christoph Weder
Publication year - 2019
Publication title -
acs macro letters
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.966
H-Index - 92
ISSN - 2161-1653
DOI - 10.1021/acsmacrolett.9b00710
Subject(s) - materials science , monomer , glass transition , polymer , phase (matter) , supramolecular chemistry , supramolecular polymers , composite material , chemical engineering , polymer chemistry , crystallography , crystal structure , organic chemistry , chemistry , engineering
A modular approach for the design of two-component supramolecular polymer (SMP) networks is reported. A series of materials was prepared by blending two (macro)monomers based on trifunctional poly(propylene oxide) (PPO) cores that were end-functionalized with hydrogen-bonding 2-ureido-4[1 H ]pyrimidinone (UPy) groups. One monomer was based on a PPO core with a number-average molecular weight ( M n ) of 440 g mol -1 . The SMP formed by this building block is a glassy, brittle material with a glass transition temperature ( T g ) of about 86 °C. The second monomer featured a PPO core with an M n of 3000 g mol -1 . The SMP formed by this building block adopts a microphase-segregated morphology that features a rubbery phase with a T g of -58 °C and crystalline domains formed by the UPy assemblies, which act as physical cross-links and melt around 90-130 °C. Combining the two components allows access to microphase-segregated blends comprised of a rubbery phase constituted by the high- M n cores, a glassy phase formed by the low- M n component, and a crystalline phase formed by UPy groups. This allowed tailoring of the mechanical properties and afforded materials with storage moduli of 37-609 MPa, tensile strengths of 2.0-5.4 MPa, and melt viscosities of as low as 11 Pa s at 140 °C. The materials can be used as reversible adhesives.
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